Altered regulation of IL-6 production with normal aging. Possible linkage to the age-associated decline in dehydroepiandrosterone and its sulfated derivative
Abstract
Normal aging in humans has been recently shown to be accompanied by reduced control over production of the multifunctional cytokine IL-6. This cytokine was reported to be quantitatively elevated in most serum samples obtained from "normal" elderly humans. In the present investigation, we report that IL-6 levels are elevated in serum samples obtained from aged mice, and its spontaneous production could also be easily detected in culture supernatants of unstimulated lymphoid cells obtained from aged, but not mature, adult donors. Spontaneous production of IL-6 was consistently observed in culture supernatants of lymphoid cells from both the spleen and mesenteric lymph nodes from aged donors, but was absent from supernatants derived from their peripheral lymph nodes. In aged mice, the reduced regulation of IL-6 production could be effectively prevented and/or reversed by supplementing aging animals with dehydroepiandrosterone sulfate, a steroid hormone whose endogenous production is known to decline with advancing age in all species tested. It was also established that serum obtained from old dehydroepiandrosterone sulfate-treated mice contained lower (normal) levels of serum amyloid P substance (an acute phase reactant), reduced levels of serum Ig (all classes and isotypes) and lower titers of tissue-specific autoantibodies than untreated aged controls. Therefore, a number of well described, age-related conditions, some of which could be contributing to the pathologic phenotype…
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IL-6 levels increase with age.
“Consistently, IL-6 levels increase with age (296, 297).”
From IL-6 in inflammation, autoimmunity and cancer (2021) · cites this paper as [296]
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References 47 · Cited by 1,264
- Authors
- Daynes, R. A., Araneo, B. A., Ershler, W. B., Maloney, C., Li, G. Z., & Ryu, S. Y.
- Affiliations
- University of Utah (US)
- ORCID
- Venue
- The Journal of Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 1993-06
- Volume
- 150
- Issue
- 12
- Pages
- 5219-5230
- ISSN
- 0022-1767 (ISSN-L)
- 1550-6606
- OpenAlex
- W2115914792
- Cited by
- 1,264
- References
- 47
- Citations by year
- 2026: 1 · 2025: 29 · 2024: 91 · 2023: 113 · 2022: 121 · 2021: 120 · 2020: 103 · 2019: 87 · 2018: 77 · 2017: 60 · 2016: 48 · 2015: 35 · 2014: 19 · 2013: 16 · 2012: 12
- FWCI
- 8.72
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Immunology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01ca033065-11, 5r01ag011475-04)
- National Institute on Aging (AG11475)
- National Cancer Institute (CA33065, CA 25917)
- Topics
- Health Sciences › Medicine › Oncology › Cytokine Signaling Pathways and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- interleukin-6, aging, dehydroepiandrosterone sulfate, spontaneous cytokine production, lymphoid cells, serum amyloid P component, immunoglobulins, autoantibodies, acute phase proteins, aged mice, age-related immunosenescence
- MeSH terms
- Aged, Aged, 80 and over, Aging, Animals, Dehydroepiandrosterone, Female, Humans, Immunoglobulins, Male, Mice, Inbred BALB C, Mice, Inbred C3H, Middle Aged, Interleukin-6, Dehydroepiandrosterone Sulfate, Mice
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